A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529086



Internal ID22398479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92917808..92917896hg38UCSC Ensembl
chr7:92547122..92547210hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8647n152
Supporting Variantsnssv14336066, nssv14336068, nssv14336069, nssv14336065, nssv14336067
SamplesHG00512, NA19238, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529086
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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